510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K924009Substantially Equivalent

Intravascular Guide Wire and Extension Wire

Pilot Cardiovascular Systems, Inc., Sub. C.R. Bard, San Clemente CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K924009 is the FDA 510(k) clearance record for INTRAVASCULAR GUIDE WIRE AND EXTENSION WIRE, a class II device, cleared for Pilot Cardiovascular Systems, Inc., Sub. C.R. Bard on under FDA product code DQX (Wire, Guide, Catheter). FDA records list 2 510(k) clearances for Pilot Cardiovascular Systems, Inc., Sub. C.R. Bard, from to . As of , FDA records show no recalls naming K924009.

Clearance record

Decision date
Received
(88 days to decision)
Product code
DQX Wire, Guide, Catheter
Regulation
21 CFR 870.1330
Device class
Class II
Review panel
Cardiovascular
Applicant
Pilot Cardiovascular Systems, Inc., Sub. C.R. Bard 1062-F Calloe Negocio, San Clemente CA
510(k) summary
Summary
Third party review
No

Clearances, product code DQX

Trailing 12 months
12 clearances under product code DQX in the twelve months to October 2026, January 2026 the highest month at 3.
Show the numbers
Monthly 510(k) clearances under FDA product code DQX, trailing twelve months
MonthClearances
November 20251
December 20250
January 20263
February 20260
March 20263
April 20260
May 20261
June 20260
July 20262
August 20260
September 20262
October 20260